The prognostic value of DNA-ploidy in colorectal carcinoma: a prospective study.

Por Kouri, M., Pyrhönen, S., Mecklin, J. P., Järvinen, H., Laasonen, A., Franssila, K., Nordling, S.
Publicado em 1990

Comparison of CA 19-9 and carcinoembryonic antigen (CEA) levels in the serum of patients with colorectal diseases.

Por Kuusela, P., Jalanko, H., Roberts, P., Sipponen, P., Mecklin, J. P., Pitkänen, R., Mäkelä, O.
Publicado em 1984

Is gastric cancer part of the tumour spectrum of hereditary non‐polyposis colorectal cancer? A molecular genetic study

Por Gylling, A, Abdel‐Rahman, W M, Juhola, M, Nuorva, K, Hautala, E, Järvinen, H J, Mecklin, J‐P, Aarnio, M, Peltomäki, P
Publicado em 2007

Direct contact in inviting high‐risk members of hereditary colon cancer families to genetic counselling and DNA testing

Por Aktan‐Collan, K, Haukkala, A, Pylvänäinen, K, Järvinen, H J, Aaltonen, L A, Peltomäki, P, Rantanen, E, Kääriäinen, H, Mecklin, J‐P
Publicado em 2007

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.

Por Nyström-Lahti, M, Sistonen, P, Mecklin, J P, Pylkkänen, L, Aaltonen, L A, Järvinen, H, Weissenbach, J, de la Chapelle, A, Peltomäki, P
Publicado em 1994

Combination of microsatellite instability and BRAF mutation status for subtyping colorectal cancer

Por Seppälä, T T, Böhm, J P, Friman, M, Lahtinen, L, Väyrynen, V M J, Liipo, T K E, Ristimäki, A P, Kairaluoma, M V J, Kellokumpu, I H, Kuopio, T H I, Mecklin, J-P
Publicado no Br J Cancer (2015)

LKB1 exonic and whole gene deletions are a common cause of Peutz‐Jeghers syndrome

Por Volikos, E, Robinson, J, Aittomäki, K, Mecklin, J‐P, Järvinen, H, Westerman, A M, de Rooij, F W M, Vogel, T, Moeslein, G, Launonen, V, Tomlinson, I P M, Silver, A R J
Publicado em 2006

The C/C(−13910) genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population

Por Rasinperä, H, Forsblom, C, Enattah, N S, Halonen, P, Salo, K, Victorzon, M, Mecklin, J-P, Järvinen, H, Enholm, S, Sellick, G, Alazzouzi, H, Houlston, R, Robinson, J, Groop, P-H, Tomlinson, I, Schwartz, S, Aaltonen, L A, Järvelä, I
Publicado em 2005

Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer

Por Kämpjärvi, K, Mäkinen, N, Kilpivaara, O, Arola, J, Heinonen, H-R, Böhm, J, Abdel-Wahab, O, Lehtonen, H J, Pelttari, L M, Mehine, M, Schrewe, H, Nevanlinna, H, Levine, R L, Hokland, P, Böhling, T, Mecklin, J-P, Bützow, R, Aaltonen, L A, Vahteristo, P
Publicado em 2012

Identification of 33 candidate oncogenes by screening for base-specific mutations

Por Tuupanen, S, Hänninen, U A, Kondelin, J, von Nandelstadh, P, Cajuso, T, Gylfe, A E, Katainen, R, Tanskanen, T, Ristolainen, H, Böhm, J, Mecklin, J-P, Järvinen, H, Renkonen-Sinisalo, L, Andersen, C L, Taipale, M, Taipale, J, Vahteristo, P, Lehti, K, Pitkänen, E, Aaltonen, L A
Publicado em 2014

Guidelines for the clinical management of Lynch syndrome (hereditary non‐polyposis cancer)

Por Vasen, H F A, Möslein, G, Alonso, A, Bernstein, I, Bertario, L, Blanco, I, Burn, J, Capella, G, Engel, C, Frayling, I, Friedl, W, Hes, F J, Hodgson, S, Mecklin, J‐P, Møller, P, Nagengast, F, Parc, Y, Renkonen‐Sinisalo, L, Sampson, J R, Stormorken, A, Wijnen, J
Publicado em 2007

Gene expression signatures for colorectal cancer microsatellite status and HNPCC

Por Kruhøffer, M, Jensen, J L, Laiho, P, Dyrskjøt, L, Salovaara, R, Arango, D, Birkenkamp-Demtroder, K, Sørensen, F B, Christensen, L L, Buhl, L, Mecklin, J-P, Järvinen, H, Thykjaer, T, Wikman, F P, Bech-Knudsen, F, Juhola, M, Nupponen, N N, Laurberg, S, Andersen, C L, Aaltonen, L A, Ørntoft, T F
Publicado em 2005